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Showing 1 to 12 of 19 entries
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[Cancer registration in England].

Nederlands tijdschrift voor geneeskunde

MEINSMA L.
PMID: 14472240
Ned Tijdschr Geneeskd. 1962 Jul 14;106:1444-6.

No abstract available.

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MEINSMA L. [Cancer registration in England]. Ned Tijdschr Geneeskd. 1962;106:1444-6
MEINSMA, L. (1962). [Cancer registration in England]. Nederlands tijdschrift voor geneeskunde, 1061444-6.
MEINSMA, L. "[Cancer registration in England]." Nederlands tijdschrift voor geneeskunde vol. 106 (1962): 1444-6.
MEINSMA L. [Cancer registration in England]. Ned Tijdschr Geneeskd. 1962 Jul 14;106:1444-6. Dutch. PMID: 14472240.
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[Cancer in the Netherlands].

Nederlands tijdschrift voor geneeskunde

MEINSMA L.
PMID: 14472239
Ned Tijdschr Geneeskd. 1962 Sep 29;106:1942-8.

No abstract available.

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MEINSMA L. [Cancer in the Netherlands]. Ned Tijdschr Geneeskd. 1962;106:1942-8
MEINSMA, L. (1962). [Cancer in the Netherlands]. Nederlands tijdschrift voor geneeskunde, 1061942-8.
MEINSMA, L. "[Cancer in the Netherlands]." Nederlands tijdschrift voor geneeskunde vol. 106 (1962): 1942-8.
MEINSMA L. [Cancer in the Netherlands]. Ned Tijdschr Geneeskd. 1962 Sep 29;106:1942-8. Dutch. PMID: 14472239.
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Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh Syndrome.

American journal of human genetics

Lake NJ, Webb BD, Stroud DA, Richman TR, Ruzzenente B, Compton AG, Mountford HS, Pulman J, Zangarelli C, Rio M, Boddaert N, Assouline Z, Sherpa MD, Schadt EE, Houten SM, Byrnes J, McCormick EM, Zolkipli-Cunningham Z, Haude K, Zhang Z, Retterer K, Bai R, Calvo SE, Mootha VK, Christodoulou J, Rötig A, Filipovska A, Cristian I, Falk MJ, Metodiev MD, Thorburn DR.
PMID: 29625026
Am J Hum Genet. 2018 Apr 05;102(4):713. doi: 10.1016/j.ajhg.2018.03.015.

No abstract available.

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Lake NJ, Webb BD, Stroud DA, et al. Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh Syndrome. Am J Hum Genet. 2018;102(4):713doi: 10.1016/j.ajhg.2018.03.015.
Lake, N. J., Webb, B. D., Stroud, D. A., Richman, T. R., Ruzzenente, B., Compton, A. G., Mountford, H. S., Pulman, J., Zangarelli, C., Rio, M., Boddaert, N., Assouline, Z., Sherpa, M. D., Schadt, E. E., Houten, S. M., Byrnes, J., McCormick, E. M., Zolkipli-Cunningham, Z., Haude, K., Zhang, Z., Retterer, K., Bai, R., Calvo, S. E., Mootha, V. K., Christodoulou, J., Rötig, A., Filipovska, A., Cristian, I., Falk, M. J., Metodiev, M. D., & Thorburn, D. R. (2018). Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh Syndrome. American journal of human genetics, 102(4), 713. https://doi.org/10.1016/j.ajhg.2018.03.015
Lake, Nicole J, et al. "Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh Syndrome." American journal of human genetics vol. 102,4 (2018): 713. doi: https://doi.org/10.1016/j.ajhg.2018.03.015
Lake NJ, Webb BD, Stroud DA, Richman TR, Ruzzenente B, Compton AG, Mountford HS, Pulman J, Zangarelli C, Rio M, Boddaert N, Assouline Z, Sherpa MD, Schadt EE, Houten SM, Byrnes J, McCormick EM, Zolkipli-Cunningham Z, Haude K, Zhang Z, Retterer K, Bai R, Calvo SE, Mootha VK, Christodoulou J, Rötig A, Filipovska A, Cristian I, Falk MJ, Metodiev MD, Thorburn DR. Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh Syndrome. Am J Hum Genet. 2018 Apr 05;102(4):713. doi: 10.1016/j.ajhg.2018.03.015. PMID: 29625026; PMCID: PMC5985357.
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Entanglement of dark electron-nuclear spin defects in diamond.

Nature communications

Degen MJ, Loenen SJH, Bartling HP, Bradley CE, Meinsma AL, Markham M, Twitchen DJ, Taminiau TH.
PMID: 34108455
Nat Commun. 2021 Jun 09;12(1):3470. doi: 10.1038/s41467-021-23454-9.

A promising approach for multi-qubit quantum registers is to use optically addressable spins to control multiple dark electron-spin defects in the environment. While recent experiments have observed signatures of coherent interactions with such dark spins, it is an open...

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Degen MJ, Loenen SJH, Bartling HP, et al. Entanglement of dark electron-nuclear spin defects in diamond. Nat Commun. 2021;12(1):3470doi: 10.1038/s41467-021-23454-9.
Degen, M. J., Loenen, S. J. H., Bartling, H. P., Bradley, C. E., Meinsma, A. L., Markham, M., Twitchen, D. J., & Taminiau, T. H. (2021). Entanglement of dark electron-nuclear spin defects in diamond. Nature communications, 12(1), 3470. https://doi.org/10.1038/s41467-021-23454-9
Degen, M J, et al. "Entanglement of dark electron-nuclear spin defects in diamond." Nature communications vol. 12,1 (2021): 3470. doi: https://doi.org/10.1038/s41467-021-23454-9
Degen MJ, Loenen SJH, Bartling HP, Bradley CE, Meinsma AL, Markham M, Twitchen DJ, Taminiau TH. Entanglement of dark electron-nuclear spin defects in diamond. Nat Commun. 2021 Jun 09;12(1):3470. doi: 10.1038/s41467-021-23454-9. PMID: 34108455; PMCID: PMC8190113.
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Current-induced magnetization reversal in high magnetic fields in Co/Cu/Co nanopillars.

Physical review letters

Ozyilmaz B, Kent AD, Monsma D, Sun JZ, Rooks MJ, Koch RH.
PMID: 12935107
Phys Rev Lett. 2003 Aug 08;91(6):067203. doi: 10.1103/PhysRevLett.91.067203. Epub 2003 Aug 08.

Current-induced magnetization dynamics in Co/Cu/Co trilayer nanopillars (approximately 100 nm in diameter) have been studied experimentally at low temperatures for large applied fields perpendicular to the layers. At 4.2 K an abrupt and hysteretic increase in resistance is observed...

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Ozyilmaz B, Kent AD, Monsma D, et al. Current-induced magnetization reversal in high magnetic fields in Co/Cu/Co nanopillars. Phys Rev Lett. 2003;91(6):067203doi: 10.1103/PhysRevLett.91.067203.
Ozyilmaz, B., Kent, A. D., Monsma, D., Sun, J. Z., Rooks, M. J., & Koch, R. H. (2003). Current-induced magnetization reversal in high magnetic fields in Co/Cu/Co nanopillars. Physical review letters, 91(6), 067203. https://doi.org/10.1103/PhysRevLett.91.067203
Ozyilmaz, B, et al. "Current-induced magnetization reversal in high magnetic fields in Co/Cu/Co nanopillars." Physical review letters vol. 91,6 (2003): 067203. doi: https://doi.org/10.1103/PhysRevLett.91.067203
Ozyilmaz B, Kent AD, Monsma D, Sun JZ, Rooks MJ, Koch RH. Current-induced magnetization reversal in high magnetic fields in Co/Cu/Co nanopillars. Phys Rev Lett. 2003 Aug 08;91(6):067203. doi: 10.1103/PhysRevLett.91.067203. Epub 2003 Aug 08. PMID: 12935107.
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Dihydropyrimidine Dehydrogenase Deficiency: Homozygosity for an Extremely Rare Variant in DPYD due to Uniparental Isodisomy of Chromosome 1.

JIMD reports

van Kuilenburg ABP, Meijer J, Meinsma R, Pérez-Dueñas B, Alders M, Bhuiyan ZA, Artuch R, Hennekam RCM.
PMID: 30349988
JIMD Rep. 2019;45:65-69. doi: 10.1007/8904_2018_138. Epub 2018 Oct 23.

Dihydropyrimidine dehydrogenase (DPD) deficiency is a rare autosomal recessive disorder of the pyrimidine degradation pathway and can lead to intellectual disability, motor retardation, and seizures. Genetic variations in DPYD have also emerged as predictive risk factors for severe toxicity...

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van Kuilenburg ABP, Meijer J, Meinsma R, et al. Dihydropyrimidine Dehydrogenase Deficiency: Homozygosity for an Extremely Rare Variant in DPYD due to Uniparental Isodisomy of Chromosome 1. JIMD Rep. 2018;45:65-69doi: 10.1007/8904_2018_138.
van Kuilenburg, A. B. P., Meijer, J., Meinsma, R., Pérez-Dueñas, B., Alders, M., Bhuiyan, Z. A., Artuch, R., & Hennekam, R. C. M. (2019). Dihydropyrimidine Dehydrogenase Deficiency: Homozygosity for an Extremely Rare Variant in DPYD due to Uniparental Isodisomy of Chromosome 1. JIMD reports, 4565-69. https://doi.org/10.1007/8904_2018_138
van Kuilenburg, André B P, et al. "Dihydropyrimidine Dehydrogenase Deficiency: Homozygosity for an Extremely Rare Variant in DPYD due to Uniparental Isodisomy of Chromosome 1." JIMD reports vol. 45 (2019): 65-69. doi: https://doi.org/10.1007/8904_2018_138
van Kuilenburg ABP, Meijer J, Meinsma R, Pérez-Dueñas B, Alders M, Bhuiyan ZA, Artuch R, Hennekam RCM. Dihydropyrimidine Dehydrogenase Deficiency: Homozygosity for an Extremely Rare Variant in DPYD due to Uniparental Isodisomy of Chromosome 1. JIMD Rep. 2019;45:65-69. doi: 10.1007/8904_2018_138. Epub 2018 Oct 23. PMID: 30349988; PMCID: PMC6336675.
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Publisher's note. Identification of a novel synonymous mutation in the human β-ureidopropionase gene UPB1 affecting pre-mRNA splicing.

Nucleosides, nucleotides & nucleic acids

Meijer J, Nakajima Y, Zhang C, Meinsma R, Ito T, Van Kuilenburg AB.
PMID: 24940676
Nucleosides Nucleotides Nucleic Acids. 2014;33(4):639-45. doi: 10.1080/15257770.2014.913907.

β-Ureidopropionase is the third enzyme of the pyrimidine degradation pathway and it catalyzes the conversion of N-carbamyl-β-alanine and N-carbamyl-β-aminoisobutyric acid to β-alanine and β-aminoisobutyric acid, respectively, and ammonia and CO2. To date, only 16 genetically confirmed patients with a...

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Meijer J, Nakajima Y, Zhang C, et al. Publisher's note. Identification of a novel synonymous mutation in the human β-ureidopropionase gene UPB1 affecting pre-mRNA splicing. Nucleosides Nucleotides Nucleic Acids. 2014;33(4):639-45doi: 10.1080/15257770.2014.913907.
Meijer, J., Nakajima, Y., Zhang, C., Meinsma, R., Ito, T., & Van Kuilenburg, A. B. (2014). Publisher's note. Identification of a novel synonymous mutation in the human β-ureidopropionase gene UPB1 affecting pre-mRNA splicing. Nucleosides, nucleotides & nucleic acids, 33(4), 639-45. https://doi.org/10.1080/15257770.2014.913907
Meijer, J, et al. "Publisher's note. Identification of a novel synonymous mutation in the human β-ureidopropionase gene UPB1 affecting pre-mRNA splicing." Nucleosides, nucleotides & nucleic acids vol. 33,4 (2014): 639-45. doi: https://doi.org/10.1080/15257770.2014.913907
Meijer J, Nakajima Y, Zhang C, Meinsma R, Ito T, Van Kuilenburg AB. Publisher's note. Identification of a novel synonymous mutation in the human β-ureidopropionase gene UPB1 affecting pre-mRNA splicing. Nucleosides Nucleotides Nucleic Acids. 2014;33(4):639-45. doi: 10.1080/15257770.2014.913907. PMID: 24940676.
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Erratum to: The potential effectiveness of the nutrition improvement program on infant and young child feeding and nutritional status in the Northwest and Southwest regions of Cameroon, Central Africa.

BMC health services research

Reinsma K, Nkuoh G, Nshom E.
PMID: 28235405
BMC Health Serv Res. 2017 Feb 24;17(1):165. doi: 10.1186/s12913-017-2109-3.

No abstract available.

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Reinsma K, Nkuoh G, Nshom E. Erratum to: The potential effectiveness of the nutrition improvement program on infant and young child feeding and nutritional status in the Northwest and Southwest regions of Cameroon, Central Africa. BMC Health Serv Res. 2017;17(1):165doi: 10.1186/s12913-017-2109-3.
Reinsma, K., Nkuoh, G., & Nshom, E. (2017). Erratum to: The potential effectiveness of the nutrition improvement program on infant and young child feeding and nutritional status in the Northwest and Southwest regions of Cameroon, Central Africa. BMC health services research, 17(1), 165. https://doi.org/10.1186/s12913-017-2109-3
Reinsma, Kate, et al. "Erratum to: The potential effectiveness of the nutrition improvement program on infant and young child feeding and nutritional status in the Northwest and Southwest regions of Cameroon, Central Africa." BMC health services research vol. 17,1 (2017): 165. doi: https://doi.org/10.1186/s12913-017-2109-3
Reinsma K, Nkuoh G, Nshom E. Erratum to: The potential effectiveness of the nutrition improvement program on infant and young child feeding and nutritional status in the Northwest and Southwest regions of Cameroon, Central Africa. BMC Health Serv Res. 2017 Feb 24;17(1):165. doi: 10.1186/s12913-017-2109-3. PMID: 28235405; PMCID: PMC5326491.
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Differences in Spontaneous Interactions of Autistic Children in an Interaction With an Adult and Humanoid Robot.

Frontiers in robotics and AI

Schadenberg BR, Reidsma D, Heylen DKJ, Evers V.
PMID: 33501197
Front Robot AI. 2020 Mar 05;7:28. doi: 10.3389/frobt.2020.00028. eCollection 2020.

Robots are promising tools for promoting engagement of autistic children in interventions and thereby increasing the amount of learning opportunities. However, designing deliberate robot behavior aimed at engaging autistic children remains challenging. Our current understanding of what interactions with...

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Schadenberg BR, Reidsma D, Heylen DKJ, et al. Differences in Spontaneous Interactions of Autistic Children in an Interaction With an Adult and Humanoid Robot. Front Robot AI. 2020;7:28doi: 10.3389/frobt.2020.00028.
Schadenberg, B. R., Reidsma, D., Heylen, D. K. J., & Evers, V. (2020). Differences in Spontaneous Interactions of Autistic Children in an Interaction With an Adult and Humanoid Robot. Frontiers in robotics and AI, 728. https://doi.org/10.3389/frobt.2020.00028
Schadenberg, Bob R, et al. "Differences in Spontaneous Interactions of Autistic Children in an Interaction With an Adult and Humanoid Robot." Frontiers in robotics and AI vol. 7 (2020): 28. doi: https://doi.org/10.3389/frobt.2020.00028
Schadenberg BR, Reidsma D, Heylen DKJ, Evers V. Differences in Spontaneous Interactions of Autistic Children in an Interaction With an Adult and Humanoid Robot. Front Robot AI. 2020 Mar 05;7:28. doi: 10.3389/frobt.2020.00028. eCollection 2020. PMID: 33501197; PMCID: PMC7805683.
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The evaluation of the integral absorbed dose in diagnostic roentgenology.

Medicamundi

REINSMA K.
PMID: 14437199
Medicamundi. 1959;5:41-6.

No abstract available.

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REINSMA K. The evaluation of the integral absorbed dose in diagnostic roentgenology. Medicamundi. 1959;5:41-6
REINSMA, K. (1959). The evaluation of the integral absorbed dose in diagnostic roentgenology. Medicamundi, 541-6.
REINSMA, K. "The evaluation of the integral absorbed dose in diagnostic roentgenology." Medicamundi vol. 5 (1959): 41-6.
REINSMA K. The evaluation of the integral absorbed dose in diagnostic roentgenology. Medicamundi. 1959;5:41-6. PMID: 14437199.
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Developing a Reliable Testing Protocol for the Hydra-Fitness Upper Body OmniTron.

The Journal of orthopaedic and sports physical therapy

Russel JA, Strong L, Meins JD.
PMID: 18780993
J Orthop Sports Phys Ther. 1992;16(2):87-91. doi: 10.2519/jospt.1992.16.2.87.

Evaluation of the reliability of musculoskeletal testing equipment is an important step in establishing the usefulness of an assessment device's data. The purposes of this study were to determine the reliability of a specific upper body OmniTron testing protocol...

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Russel JA, Strong L, Meins JD. Developing a Reliable Testing Protocol for the Hydra-Fitness Upper Body OmniTron. J Orthop Sports Phys Ther. 1992;16(2):87-91doi: 10.2519/jospt.1992.16.2.87.
Russel, J. A., Strong, L., & Meins, J. D. (1992). Developing a Reliable Testing Protocol for the Hydra-Fitness Upper Body OmniTron. The Journal of orthopaedic and sports physical therapy, 16(2), 87-91. https://doi.org/10.2519/jospt.1992.16.2.87
Russel, J A, et al. "Developing a Reliable Testing Protocol for the Hydra-Fitness Upper Body OmniTron." The Journal of orthopaedic and sports physical therapy vol. 16,2 (1992): 87-91. doi: https://doi.org/10.2519/jospt.1992.16.2.87
Russel JA, Strong L, Meins JD. Developing a Reliable Testing Protocol for the Hydra-Fitness Upper Body OmniTron. J Orthop Sports Phys Ther. 1992;16(2):87-91. doi: 10.2519/jospt.1992.16.2.87. PMID: 18780993.
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Dihydropyrimidine Dehydrogenase Deficiency: Metabolic Disease or Biochemical Phenotype?.

JIMD reports

Fleger M, Willomitzer J, Meinsma R, Alders M, Meijer J, Hennekam RCM, Huemer M, van Kuilenburg ABP.
PMID: 28275972
JIMD Rep. 2017;37:49-54. doi: 10.1007/8904_2017_14. Epub 2017 Mar 09.

Dihydropyrimidine dehydrogenase (DPD) deficiency is an autosomal recessive disorder of pyrimidine metabolism that impairs the first step of uracil und thymine degradation. The spectrum of clinical presentations in subjects with the full biochemical phenotype of DPD deficiency ranges from...

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Fleger M, Willomitzer J, Meinsma R, et al. Dihydropyrimidine Dehydrogenase Deficiency: Metabolic Disease or Biochemical Phenotype?. JIMD Rep. 2017;37:49-54doi: 10.1007/8904_2017_14.
Fleger, M., Willomitzer, J., Meinsma, R., Alders, M., Meijer, J., Hennekam, R. C. M., Huemer, M., & van Kuilenburg, A. B. P. (2017). Dihydropyrimidine Dehydrogenase Deficiency: Metabolic Disease or Biochemical Phenotype?. JIMD reports, 3749-54. https://doi.org/10.1007/8904_2017_14
Fleger, M, et al. "Dihydropyrimidine Dehydrogenase Deficiency: Metabolic Disease or Biochemical Phenotype?." JIMD reports vol. 37 (2017): 49-54. doi: https://doi.org/10.1007/8904_2017_14
Fleger M, Willomitzer J, Meinsma R, Alders M, Meijer J, Hennekam RCM, Huemer M, van Kuilenburg ABP. Dihydropyrimidine Dehydrogenase Deficiency: Metabolic Disease or Biochemical Phenotype?. JIMD Rep. 2017;37:49-54. doi: 10.1007/8904_2017_14. Epub 2017 Mar 09. PMID: 28275972; PMCID: PMC5740048.
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